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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474351Generated: October 29, 2026

Thioacetamide → Ethyl 2-methyl-4-(2-methylphenyl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/474351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioacetamideHCID 2723949—
Reactant2-Bromo-3-oxo-3-o-tolyl-propionic acid ethyl esterHCID 22437388—
SolventEthanolHCID 702—
ProductEthyl 2-methyl-4-(2-methylphenyl)-1,3-thiazole-5-carboxylateHCID 5344088834%

Reaction Steps

A stirred mixture of 2-bromo-3-oxo-3-o-tolyl-propionic acid ethyl ester (2.74 g, 9.60 mmol, 1.0 equiv) and thioacetamide (0.76 g, 10.1 mmol, 1.05 equiv) in ethanol (30 mL) was heated to reflux for 4 hours. The cooled mixture was filtered and concentrated under vacuum. The residue was partitioned between ethyl acetate and water and the organic phase was separated and then washed with saturated aqueous sodium chloride solution. The collected organic was dried over magnesium sulphate, filtered, and concentrated under vacuum. The resultant residue was purified by flash column chromatography on silica gel (gradient: 0 to 20% ethyl acetate in pentane) to afford 0.84 g (34%) of 2-methyl-4-o-tolyl-thiazole-5-carboxylic acid ethyl ester as an oil. LCMS (ESI) m+H=261.9; 1H NMR (400 MHz, CDCl3) δ: 7.31-7.18 (m, 4H), 4.16 (q, 2H), 2.76 (s, 3H), 2.18 (s, 3H), 1.14 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637526B2
Source datasetuspto-grants-2014_01
ORD IDord-d8696266c6da46af8659fd8e3f03da8f
Source noteuspto-grants-2014_01